A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526966



Internal ID15107573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43302843..43366735hg38UCSC Ensembl
Innerchr19:43806995..43870887hg19UCSC Ensembl
Innerchr19:48498835..48562727hg18UCSC Ensembl
Innerchr19:48498835..48562727hg17UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3863893
hg1963893
hg1863893
hg1763893
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703338
Samples
Known GenesCD177, PRG1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526966
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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